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致心律失常性心肌病的运动处方:在风险与益处之间找到恰当平衡

Exercise Prescription in Arrhythmogenic Cardiomyopathy: Finding the Right Balance Between Risks and Benefits.

作者信息

Dei Lorenzo-Lupo, Han Jennie, Romano Silvio, Sciarra Luigi, Asimaki Angeliki, Papadakis Michael, Sharma Sanjay, Finocchiaro Gherardo

机构信息

Department of Life, Health and Environmental Sciences University of L'Aquila Italy.

Cardiovascular Sciences Research Centre, St George's University of London UK.

出版信息

J Am Heart Assoc. 2025 Jun 17;14(12):e039125. doi: 10.1161/JAHA.124.039125. Epub 2025 Jun 5.

DOI:10.1161/JAHA.124.039125
PMID:40470644
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12229179/
Abstract

Arrhythmogenic cardiomyopathy (ACM) is an inherited cardiac condition, often caused by mutations in genes encoding desmosomal proteins. The pathologic hallmark of the disease is a fibrofatty replacement of the myocardium, which constitutes the substrate for potentially fatal ventricular arrhythmias. ACM is one of the most common etiology of sudden cardiac death in athletes and young individuals. Although it is well established that regular exercise confers multiple health benefits and better survival in the general population, intense exercise may accelerate the phenotypic expression and the propensity to ventricular arrhythmias in patients with ACM. This review discusses current evidence regarding the safety and the effects of exercise in ACM. We scrutinize research findings based on animal and human models that raise concerns on the possible detrimental role of intense exercise in this condition. Finally, we examine the current knowledge on exercise prescription focusing on the optimal amount of exercise that should be recommended to patients with ACM.

摘要

致心律失常性心肌病(ACM)是一种遗传性心脏疾病,通常由编码桥粒蛋白的基因突变引起。该病的病理标志是心肌的纤维脂肪替代,这构成了潜在致命性室性心律失常的基础。ACM是运动员和年轻人心脏性猝死最常见的病因之一。虽然普遍认为规律运动对健康有益且能提高总体人群的生存率,但剧烈运动可能会加速ACM患者的表型表达以及室性心律失常的发生倾向。本综述讨论了当前关于ACM患者运动安全性和影响的证据。我们仔细研究了基于动物和人体模型的研究结果,这些结果引发了对剧烈运动在这种情况下可能产生的有害作用的担忧。最后,我们审视了当前关于运动处方的知识,重点关注应推荐给ACM患者的最佳运动量。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/44f4/12229179/6111356e07fd/JAH3-14-e039125-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/44f4/12229179/337d8b2907e0/JAH3-14-e039125-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/44f4/12229179/444c52f439dc/JAH3-14-e039125-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/44f4/12229179/1c7f5022d098/JAH3-14-e039125-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/44f4/12229179/6111356e07fd/JAH3-14-e039125-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/44f4/12229179/337d8b2907e0/JAH3-14-e039125-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/44f4/12229179/444c52f439dc/JAH3-14-e039125-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/44f4/12229179/1c7f5022d098/JAH3-14-e039125-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/44f4/12229179/6111356e07fd/JAH3-14-e039125-g002.jpg

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